← Back to catalogue

Premier SENSIPAST

FDA UDI

Class I (US FDA UDI)

by Premier Dental Products Company

Identity

Trade Name
Premier SENSIPAST FDA UDI
Generic Name
Endodontic obturation material distribution endpiece, reusable FDA UDI
Device Name
FILLER SENSIPAST PKG4 21MM 25 FDA UDI
Model / Reference
9053571 FDA UDI
Description
FILLER SENSIPAST PKG4 21MM 25 FDA UDI

Identifiers

Primary DI / UDI-DI
D6919053571 FDA UDI
FDA Product Code
EIY FDA UDI
GMDN Term
Endodontic obturation material distribution endpiece, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Endodontic obturation material distribution endpiece, reusable

Premier SENSIPAST by Premier Dental Products Company — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endodontic obturation material distribution endpiece, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Premier Dental Products Company

Sources (1)

  • FDA UDI 1df4e4ed-891e-46b8-97e2-a6b2d26ad77c 33 fields · synced Jun 8, 2026